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Clinical Trials/NCT05365464
NCT05365464
Withdrawn
Phase 2

hCG or Progesterone Effect on Unexplained Recurrent Pregnancy Loss

Overview

Phase
Phase 2
Intervention
Progesterone Pill
Conditions
Recurrent Pregnancy Loss Without Current Pregnancy
Sponsor
Wake Forest University Health Sciences
Primary Endpoint
Miscarriage
Status
Withdrawn
Last Updated
3 years ago

Overview

Brief Summary

Up to half of all cases of recurrent pregnancy loss are unexplained (uRPL). Evidence points towards endometriosis and progesterone resistance as an underlying cause of uRPL. Previous non-RCT studies have suggested the luteal hCG provides a useful treatment for uRPL. We propose performing a randomized controlled trial to compare mid-luteal hCG with oral progesterone to prevent early pregnancy losses. the endpoint will be ongoing pregnancy and live birth rates. Equal numbers of patients will be randomized to each group.

Detailed Description

Fifty (50) patients with unexplained recurrent pregnancy loss, defined as 2 or more losses. Workup will exclude structural, genetic, hormonal, and anti-phospholipid syndrome-related causes of RPL. Women with unexplained RPL will be randomized to receive a mid-luteal injection of ovidril (250 ug) 1 week after ovulation vs prometrium (200 mg qhs) starting 4 days after ovulation. If pregnant, prometrium will be continued until 8 weeks of pregnancy. If pregnancy does not occur, subjects will be allowed to repeat this protocol for up to 3 cycles. Outcomes will be listed as "not pregnant", "biochemical pregnancy", "miscarriage" or "ongoing pregnancy" for each cycle. Endpoints of pregnant cycles will be compared for pregnancy rate, miscarriage rate, ongoing pregnancy rate and live birth rate.

Registry
clinicaltrials.gov
Start Date
May 2022
End Date
December 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 2 first trimester losses
  • unexplained recurrent pregnancy loss

Exclusion Criteria

  • Antiphospholipid syndrome
  • uterine septum
  • Asherman's syndrome
  • Paternal or maternal genetic abnormalities (i.e. balanced translocation)
  • Endocrine causes of RPL (thyroid, diabetes, hyperprolactinemia)

Arms & Interventions

Progesterone

Women receive prometrium 200 mg qhs for up to 8 weeks

Intervention: Progesterone Pill

hCG

A single shot of hCG (ovidril 250 ug) will be given as a subcutaneous injection 1 week after ovulation

Intervention: hCG

Outcomes

Primary Outcomes

Miscarriage

Time Frame: 4 to 11 weeks

Loss of pregnancy before 11 weeks of pregnancy

Ongoing pregnancy

Time Frame: 8 weeks

Successgful pregnancy beyond 8 weeks of gestation with a heart beat

Secondary Outcomes

  • Live birth rate(40 weeks)

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